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EBook For Oxadiazole in Material and Medicinal Chemistry 1st Edition By Sahoo P.R, Saxena A., Kumar S
Original price was: $100.00.$20.00Current price is: $20.00.
- ISBN-10 : 1032470666
- ISBN-13 : 978-1032470665
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EBook For Oxadiazole in Material and Medicinal Chemistry 1st Edition By Sahoo P.R, Saxena A., Kumar S
Table Of Content
- Contents
- 1 Diverse Synthetic Approaches to Design and Develop Oxadiazole-Based Heterocyclic Scaffolds
- 1 Introduction
- 2 Synthesis of 1,2,4-Oxadiazole Derivatives
- 2.1 Coupling Agent Assisted 1,2,4-Oxadiazole Synthesis
- 2.2 Pd Catalyzed Oxadiazole Synthesis
- 2.3 Solid Phase-Based Synthesis of 1,2,4-Oxadiazole Derivative
- 2.4 1,2,4-Oxadiazole Synthesis Using Oxidants
- 2.5 Visible Light Promoted 1,2,4-Oxadiazole Synthesis
- 3 Synthesis of 1,3,4-Oxadiazole Derivatives
- 3.1 POCl3-Promoted Oxadiazole Synthesis
- 3.2 Pd Catalyzed Oxadiazole Synthesis
- 3.3 Microwave-Assisted Synthesis
- 3.4 Solid Phase-Based Synthesis of 1,3,4-Oxadiazole Derivative
- 3.5 Iodine-Promoted Synthesis of 1,3,4-Oxadiazole Derivative
- 3.6 1,3,4-Oxadiazole Synthesis Using Oxidants
- 3.7 Visible Light Promoted 1,3,4-Oxadiazole Synthesis
- 3.8 Polymer-Based 1,3,4-Oxadiazole Derivative Synthesis
- 3.9 Other Methods for Synthesis of 1,3,4-Oxadiazole Derivative
- 4 Conclusions
- References
- 2 1,2,4 and 1,3,4-Oxadiazole Scaffolds in Designing Organic Light-Emitting Diodes
- 1 Introduction
- 2 Organic Light-Emitting Diodes Based on 1,2,4-Oxadiazole Derivatives
- 3 Organic Light-Emitting Diodes Based on 1,3,4-Oxadiazole Derivatives
- 4 Metal Complex-Based Oxadiazole Systems
- 5 Polymer-Based Oxadiazole Systems
- 6 Conclusions
- References
- 3 Oxadiazole as Liquid Crystals
- 1 Introduction
- 2 Classification of Liquid Crystals
- 3 Classification of Liquid Crystalline Phases
- 4 Oxadiazole as Liquid Crystals
- 5 Mesomorphic Features
- 6 Conclusion
- References
- 4 Oxadiazole as Electrochromic Materials
- 1 Introduction
- 2 Mechanism of Electrochromism
- 3 Advantages of Oxadiazole as Electrochromic Materials
- 3.1 Oxadiazole in Combination With Polythiophene
- 3.2 Oxadiazole in Combination With TTF Derivatives
- 3.3 Oxadiazole in Combination With Carbazole Derivatives
- 3.4 Oxadiazole in Combination With Organic Amines
- 3.5 Oxadiazole in Combination With Fluorene
- 4 Conclusion
- References
- 5 Oxadiazole as Nonlinear Optical (NLO) Materials
- 1 Introduction
- 2 Oxadiazole Derivatives With Donor-Acceptor Properties
- 2.1 Polyacetylenes Containing Oxadiazole Pendant Groups
- 2.2 Polyacetylenes Containing Oxadiazole and Thiophene Pendant Groups
- 2.3 Poly(3,4-Dialkoxythiophene)s-1,3,4-Oxadiazole Derivative Conjugates
- 2.4 Oxadiazole-Bisphenol Conjugates
- 3 Conclusion
- References
- 6 Oxadiazole-Based Heterocyclic Compounds as Chemical Probes in Live Cell Imaging
- 1 Introduction
- 2 Oxadiazole-Based Probes in PET Imaging
- 3 Oxadiazole-Based Probes for SPECT Imaging
- 4 Oxadiazole-Based Probes as Enzyme Markers
- 5 Oxadiazole-Based Probes in Protein Imaging
- 6 Nitric Oxide Imaging
- 7 Oxadiazole-Based Probes for Metal Ion Imaging
- 7.1 Al3+ Imaging
- 7.2 Ca2+ Imaging
- 7.3 Fe2+/3+ Imaging
- 7.4 Zn2+ Imaging
- 8 Oxadiazole-Based Probes for pH Imaging
- 9 Oxadiazole-Based Probes in Cell Imaging and Nrf2 Activation
- 10 Conclusions
- References
- 7 Oxadiazole as Inhibitors
- 1 Introduction
- 1 The Derivatized Compound From Oxadiazole: A Potential Inhibitor
- 2.1 Inhibitors as Anti-Methicillin-Resistant Staphylococcus aureus (MRSA) Agents
- 2.2 Inhibitors Against MRSA as Antibacterial Agents
- 3 Role of Histone Deacetylase (HDAC) Inhibitors in Anticancer Therapy
- 4 Conclusion
- References
- 8 Oxadiazole in Medicine and Drug Discovery
- 1 Introduction
- 2 Different Types of Conjugates
- 2.1 Oxadiazole-Pyridine Conjugate
- 2.2 Oxadiazole-Benzofuran Conjugates
- 2.3 Oxadiazole–Thiazole Conjugates
- 2.4 Piperazine Incorporated 1,3,4–Oxadiazole Derivatives
- 2.5 Oxadiazole-Indole, Pyridine, Benzothiazole, and Benzoimidazole Conjugates
- 3 Applications
- 3.1 Antitubercular Activity
- 3.2 Antimalarial Activity
- 3.3 Anti–Inflammatory Activity
- 3.4 Anti–HIV Activity
- 3.5 Antimicrobial Activity
- 3.6 Antitumor/Anticancer/Antiproliferative Activities
- 4 Conclusion and Prospects
- References
- Index
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